Variant DetailsVariant: esv1005947Internal ID | 6718068 | Landmark | | Location Information | | Cytoband | 10q11.22 | Allele length | Assembly | Allele length | hg38 | 1107 | hg19 | 1107 | hg18 | 1107 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv3587129 | Samples | HuRef | Known Genes | ARHGAP22 | Method | Oligo aCGH | Analysis | | Platform | Not Submitted | Comments | | Reference | Pang_et_al_2010 | Pubmed ID | 20482838 | Accession Number(s) | esv1005947
| Frequency | Sample Size | 3 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
|
|